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rs281860545

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860545(A;A)
Make rs281860545(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271086
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860545
ebirs281860545
HLIrs281860545
Exacrs281860545
Varsomers281860545
Maprs281860545
PheGenIrs281860545
hapmaprs281860545
1000 genomesrs281860545
hgdprs281860545
ensemblrs281860545
gopubmedrs281860545
geneviewrs281860545
scholarrs281860545
googlers281860545
pharmgkbrs281860545
gwascentralrs281860545
openSNPrs281860545
23andMers281860545
23andMe allrs281860545
SNP Nexus

SNPshotrs281860545
SNPdbers281860545
MSV3drs281860545
GWAS Ctlgrs281860545
Max Magnitude0
ClinVar
Risk rs281860545(A;A)
Alt rs281860545(A;A)
Reference rs281860545(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238863C>T
CLNSRC
CLNACC